87820-88-0
Chemical Structure
Tralkoxydim
Synonym(s): PP604; ICIA 0604; FD-4026
- CAS No.: 87820-88-0
- Formula:C20H27NO3
- Molecular Weight:329.43
IUPAC Name: (Z)-4-(1-(ethoxyimino)propyl)-5-hydroxy-2',4',6'-trimethyl-1,6-dihydro-[1,1'-biphenyl]-3(2H)-one
InChIKey: DQFPEYARZIQXRM-PGMHBOJBSA-N
SMILES: O=C1C(/C(CC)=N\OCC)=C(O)CC(C2=C(C)C=C(C)C=C2C)C1
Biological Activity: Tralkoxydim (PP604) is an orally effective herbicide. Tralkoxydim inhibits ACCase (IC50 of 0.5 μM in Lolium rigidum), blocking ATP-dependent acetyl-CoA carboxylation to malonyl-CoA and fatty acid biosynthesis; it activates HRP-catalyzed TMB/PDA peroxidation. Tralkoxydim can be used for research on hepatic porphyria[1][2][3][4][5][6][7][8].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Tralkoxydim | 97.22% | Tralkoxydim (PP604) is an orally effective herbicide. Tralkoxydim inhibits ACCase (IC50 of 0.5 μM in Lolium rigidum), blocking ATP-dependent acetyl-CoA carboxylation to malonyl-CoA and fatty acid biosynthesis; it activates HRP-catalyzed TMB/PDA peroxidation. Tralkoxydim can be used for research on hepatic porphyria. | ||||||||||||||||||||
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Tralkoxydim (Standard) | ≥98% | Tralkoxydim (Standard) (PP604 (Standard); ICIA 0604 (Standard); FD-4026 (Standard)) is the analytical standard of Tralkoxydim (HY-111223). This product is intended for research and analytical applications. Tralkoxydim (PP604) is an orally effective herbicide. Tralkoxydim inhibits ACCase (IC50 of 0.5 μM in Lolium rigidum), blocking ATP-dependent acetyl-CoA carboxylation to malonyl-CoA and fatty acid biosynthesis; it activates HRP-catalyzed TMB/PDA peroxidation. Tralkoxydim can be used for research on hepatic porphyria. | ||||||||||||||||||||
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References
- [1]. Preston C, et al. Multiple Resistance to Dissimilar Herbicide Chemistries in a Biotype ofLolium rigidumDue to Enhanced Activity of Several Herbicide Degrading Enzymes. Pesticide Biochemistry and Physiology. 1996 Feb 1;54(2):123-34.
- [2]. Potapovich MV, et al. [Effect of herbicide tralkoxydim and 2-acylcyclohexane-1,3-diones on peroxidase activity]. Prikladnaia biokhimiia i mikrobiologiia. 2008;44(1):24-33.
- [3]. Polat E, et al. Enhanced biodiesel properties of Auxenochlorella sp. using chemical mutagenesis and Tralkoxydim. International Journal of Green Energy. 2023 Sep 2;20(11):1137-48.
- [4]. Secor J, et al. Inhibition of Acetyl-CoA Carboxylase Activity by Haloxyfop and Tralkoxydim. Plant physiology. 1988 Jan;86(1):10-2.
- [5]. Goldberg-Cavalleri A, et al. Functional Characterization of Cytochromes P450 Linked to Herbicide Detoxification and Selectivity in Winter Wheat and the Problem Competing Weed Blackgrass. ACS omega. 2025 Apr 01;10(12):12270-12287.
- [6]. Patiño-Ropero MJ, et al. Unveiling the photodegradation of tralkoxydim herbicide and its formulation in natural waters: Structural elucidation of transformation products and toxicity assessment. Ecotoxicology and environmental safety. 2025 Jul 01;299:118409.
- [7]. Guéniche N, et al. Combined in silico and in vitro approaches to identify P-glycoprotein-inhibiting pesticides. Journal of biochemical and molecular toxicology. 2024 Jan;38(1):e23588.
- [8]. Pauli BD, et al. Hepatic porphyria induced by the herbicide tralkoxydim in small mammals is species-specific. Environmental toxicology and chemistry. 2005 Feb;24(2):450-6.
